Core Technician– Cell Therapy 3rd Shift

Core Technician – Cell Therapy

Location: This is an on-site position located in Houston, TX.

As a Core Technician - Cell Therapy , you will play a critical role in the manufacturing of clinical and commercial cell therapy products within a highly regulated GMP environment. This position is responsible for performing aseptic cell processing activities, operating production equipment, completing GMP documentation, and supporting the safe and compliant manufacture of life-saving therapies. Working closely with Manufacturing, Quality, and Operational teams, you will help ensure products are produced according to established procedures, quality standards, and production schedules.

This is a competitive, hourly paid position. In addition, below you will find a comprehensive summary of the benefits package we offer:

• Performance-related bonus.
• Medical, dental and vision insurance.
• 401(k) matching plan.
• Life insurance, as well as short-term and long-term disability insurance.
• Employee assistance programs.
• Paid time off (PTO).

Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.

• Participate in the aseptic processing and manufacture of clinical and commercial cell therapy products.
• Perform aseptic cell culture manipulations within Grade A/B cleanroom environments.
• Operate cell processing and manufacturing equipment according to approved SOPs.
• Troubleshoot basic equipment issues and elevate concerns as appropriate.
• Follow contamination control and containment strategies to maintain a compliant GMP manufacturing environment.
• Participate in assigned customer Aseptic Process Simulations (APS).
• Complete GMP documentation accurately, thoroughly, and in a timely manner.
• Review manufacturing batch records (MBRs) and related GMP documentation as required.
• Adhere to all safety policies, procedures, and applicable regulations.
• Identify, document, and communicate deviations from standard procedures and accepted practices.
• Provide accurate information and support during process deviation investigations.
• Follow production schedules and execute assigned manufacturing activities efficiently.
• Collaborate effectively with Manufacturing, Quality Assurance, Quality Control, and other site functions to support operational objectives.
• Perform additional duties as assigned in support of manufacturing operations.

• High school diploma or equivalent required;
  Associate degree in a scientific or technical discipline preferred.
• 1-2 years of experience working with cell therapy technologies or related biopharmaceutical manufacturing processes in a cGMP environment.
• Working knowledge of aseptic processing principles and cleanroom operations.
• Ability to perform aseptic manipulations while maintaining product and environmental integrity.
• Ability to read, understand, and follow SOPs, manufacturing instructions, and production schedules.
• Understanding of cGMP requirements and the importance of regulatory compliance.
• Experience completing GMP documentation and reviewing manufacturing records is preferred.
• Proficiency with Microsoft Office applications, including Excel; experience with SAP and LIMS is desirable.
• Strong organizational, time management, and prioritization skills.
• Effective verbal and written communication skills.
• Ability to work collaboratively within a team environment and resolve issues professionally.
• Self-motivated, solution-oriented, and committed to operational excellence.
• Ability to perform aseptic gowning on a routine basis.
• Ability to stand for extended periods, up to 6 hours.
• Ability to routinely lift up to 50 pounds.

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